ClinVar Miner

List of variants in gene LCK reported as uncertain significance for T-B- severe combined immunodeficiency

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_005356.5(LCK):c.1016A>G (p.Asn339Ser)
NM_005356.5(LCK):c.1382G>A (p.Arg461His)
NM_005356.5(LCK):c.252G>T (p.Lys84Asn)
NM_005356.5(LCK):c.559G>A (p.Asp187Asn) rs539280346
NM_005356.5(LCK):c.601G>A (p.Gly201Ser)
NM_005356.5(LCK):c.632A>T (p.Asn211Ile)
NM_005356.5(LCK):c.803C>T (p.Thr268Met) rs1557585827
NM_005356.5(LCK):c.851C>G (p.Ala284Gly)
NM_005356.5(LCK):c.896G>A (p.Arg299Gln)
NM_005356.5(LCK):c.90G>A (p.Leu30=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.